首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Long-term faecal carriage in infants and intra-household transmission of CTX-M-15-producing Klebsiella pneumoniae following a nosocomial outbreak
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Long-term faecal carriage in infants and intra-household transmission of CTX-M-15-producing Klebsiella pneumoniae following a nosocomial outbreak

机译:在医院爆发后,婴儿的长期粪便携带婴儿和家庭内炎肺炎肺炎

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摘要

Objectives: To investigate the duration of faecal carriage of CTX-M-15-producing Klebsiella pneumoniae in infants colonized during a nosocomial neonatal intensive care unit (NICU) outbreak after discharge from hospital, possible risk factors for long-term colonization and transmission to household contacts (HCs). Methods: Fifty-one infants colonized with two unrelated clones of CTX-M-15 K. pneumoniae [sequence type (ST) 17 and ST485] during an NICU outbreak and 60 HCs provided faecal and rectal samples, respectively, every 1-3 months after hospital discharge. Extended-spectrum β-lactamase (ESBL)-producing strains of K. pneumoniae were identified on Chrom ID ESBL agar and examined by antimicrobial susceptibility testing. blaCTX-M-15 was detected by PCR and DNA sequencing. Clonal relationship was examined by PFGE. Results: The median carriage time in infants after discharge was 12.5 months (IQR 9.5-17.5). Stable antimicrobial susceptibility patterns in PFGE-related strains confirmed the intestinal persistence of both outbreak strains. Risk factors for prolonged faecal carriage in infants were delivery by caesarean section [hazard ratio (HR) 2.4, 95% CI 1.1-5.5, P = 0.029] and treatment with antibiotics during hospitalization (HR 4.5, 95% CI 1.6-12.6, P = 0.004). Transmission of CTX-M-15 K. pneumoniae was observed in 9/28 (32%) households. Median carriage length in parents was 2.5 months (IQR 1.0-5.0) (P 0.001 compared with infants). Conclusions: Infants may be long-term faecal carriers of ESBL-producing K. pneumoniae after colonization during hospitalization in the neonatal period. Delivery by caesarean section and antibiotic treatment during hospitalization are possible risk factors for prolonged carriage. Faecal ESBL carriage in infants represents a reservoir for intra-household spread of ESBL-producing K. pneumoniae.
机译:目的:探讨在医院排出后泌尿急款新生儿重症监护单位(NICU)爆发期间CTX-M-15生产Klebsiella肺炎肺炎肺炎的粪便运输的持续时间,可能是长期定植和传输到家庭的可能性因素联系人(HCS)。方法:在NICU爆发期间,用两个无关克隆的CTX-M-15K.肺炎肺炎(ST)17和ST485]中殖民殖民殖民。每1-3个月,分别为粪便和直肠样品分别提供了60 HCS出院后。扩展光谱β-内酰胺酶(ESBL) - 在ChROM ID ESBL琼脂上鉴定K.肺炎的菌株。通过抗微生物易感性测试检查。通过PCR和DNA测序检测Blactx-M-15。 PFGE检查了克隆关系。结果:排放后婴儿的中位数乘坐时间为12.5个月(IQR 9.5-17.5)。 PFGE相关菌株中稳定的抗菌易感模式证实了爆发菌株的肠持续存在。婴儿长期粪便携带的危险因素通过剖腹产段[危险比(HR)2.4,95%CI 1.1-5.5,P = 0.029]以及住院期间的抗生素(HR 4.5,95%CI 1.6-12.6,P = 0.004)。在9/28(32%)家庭中观察到CTX-M-15 K.肺炎的透射。父母中位数托架长度为2.5个月(IQR 1.0-5.0)(P <0.001与婴儿相比)。结论:婴儿可能是在新生儿期间住院期间殖民化后产生ESBL的K.肺炎的长期粪便载体。住院期间剖腹产和抗生素治疗的递送是可能的持续危险因素。婴儿粪便ESBL支架代表了ESBL-生育K.肺炎的家庭内部涂抹储层。

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  • 作者单位

    Department of Medical Microbiology Stavanger University Hospital Stavanger Norway Department of;

    Department of Paediatrics Stavanger University Hospital Stavanger Norway;

    Department of Medical Microbiology Stavanger University Hospital Stavanger Norway Department of;

    Department of Medical Biology University of Troms? Troms? Norway Department of Microbiology and;

    Department of Clinical Medicine University of Bergen Bergen Norway Department of Paediatrics;

    Department of Medical Biology University of Troms? Troms? Norway Department of Microbiology and;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
  • 关键词

    Children; Enterobacteriaceae; ESBLs; Extended-spectrum β-lactamases; Risk factors;

    机译:儿童;肠杆菌薄膜;ESBLS;扩展光谱β-内酰胺酶;危险因素;

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